510(k) Report

Devices descending from K091750

14 later devices reach Guideliner Catheter, Models 5571, 5572, 5573 through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K112100M2 Navigation Catheter and Guideliner Navigation CatheterVascular Solutions, Inc.20120—
+1K112082Guideliner V2 CatheterVascular Solutions, Inc.2011121
+2K172090GuideLiner V3 CatheterVascular Solutions, Inc.20178—
+2K161901TrapLiner catheterVascular Solutions, Inc.20171—
+2K120707Switch-IT CatheterVascular Solutions, Inc.20120—
+3K220691LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter ExtensionSeigla Medical, Inc.20221—
+3K210110GuidionImds Operations B.V.20211—
+3K183353Telescope Guide Extension CatheterMedtronic, Inc.20193—
+3K180088TrapLiner catheterVascular Solutions, Inc.20180—
+4K252390Telescope Guide Extension CatheterMedtronic, Ireland20250—
+4K242337FlowGuide (FG60F); GuidionShort (GS60F)Imds Operations B.V.20250—
+4K243691LiquID .051 LP Guide Catheter ExtensionSeigla Medical, Inc.20250—
+4K242276CrossFAST™ Integrated Microcatheter Guide Extension System (CFM55)Vantis Vascular, Inc.20241—
+5K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.20260—